Clinical trials: Anesthesia Time
Anesthesia; Adverse Effect, Spinal and Epidural
Comparative Study Between Bilateral and Unilateral Spinal Anaesthesia
The purpose of this study is to compare unilateral spinal anesthesia using hyperbaric Prilocaine with "classical bilateral spinal anesthesia" using plain Prilocaine according to block characteristics and quality of micturition…
- Trial name
- NCT01877356
- Testing
- bilateral spinal anesthesia, unilateral spinal anesthesia
- Where
- Belgium
- Volunteers
- 25 people
- Sponsor
- University Hospital, Antwerp
Intubation; Difficult or Failed, Airway Complication of Anesthesia
Comparing Full vs. Partial Glottis View Using CMAC D-Blade Video Laryngoscope in Simulated Cervical Injury Patient
Direct laryngoscope requires proper alignment of the oro-pharyngeal-laryngeal axis to provide an optimal glottic view for intubation.
- Trial name
- NCT04833166
- Testing
- CMAC D-blade videolaryngoscope with full or partial glottic view
- Where
- Malaysia
- Volunteers
- 104 people, healthy volunteers welcome
- Sponsor
- University of Malaya
Anesthesia, Local
Does Perineural Dexamethasone Increase the Duration of an Ulnar Nerve Block When Controlling for Systemic Effects?
Investigators will assess if perineural dexamethasone can increase the duration of an ulnar nerve block when controlling for systemic effects in healthy volunteers.
- Trial name
- NCT04817982
- Testing
- Perineural dexamethasone, Lidocaine, Systemic dexamethasone
- Where
- Denmark
- Volunteers
- 16 people, healthy volunteers welcome
- Sponsor
- Zealand University Hospital
Post Anesthesia Discharge Time in Patients of Breast Cancer Surgery
Effect of Dexmedetomidine Infusion on Post Anesthesia Discharge Time
A randomised control trial evaluating the effect of low dose dexmedetomidine infusion on post anesthesia discharge time in patients of day case breast cancer surgery compared with placebo infusion.
- Trial name
- NCT07180810
- Testing
- Dexmedetomidine infusion low dose, Group B receiving normal saline
- Where
- Pakistan
- Volunteers
- 82 people
- Sponsor
- Shaukat Khanum Memorial Cancer Hospital & Research Centre
Post Induction Hypotension, Postoperative Morbidity
Preoperative Carotid Doppler Ultrasound Parameters for Prediction of Post-Induction Hypotension in Elective Non-Cardiac Surgery
This prospective observational study aims to evaluate the predictive value of preoperative carotid Doppler ultrasound parameters, including carotid velocity-time integral (carotid VTI) and corrected carotid flow time (ccFT), for…
- Trial name
- NCT07488182
- Where
- Turkey (Türkiye)
- Volunteers
- 110 people
- Sponsor
- Necmettin Erbakan University
Airway Management, Tracheal Intubation
Effect of Night Shift Versus Daytime Duty on Tracheal Intubation Complications and Duration in Surgical Patients
Airway management is one of the most critical steps of anesthesia, and its complications can be life-threatening. Reduced staffing, differences in personnel experience, and physical and mental fatigue during off-hours (evenings…
- Conditions
- Airway Management, Tracheal Intubation, Intubation Complications, General Anesthesia
- Trial name
- NCT07823179
- Testing
- Tracheal Intubation
- Volunteers
- 1,000 people
- Sponsor
- Merve Yazici Kara
Spinal Anesthesia Duration
Comparison of Different Doses of Dexmedetomidine Effect in the Duration of Spinal Anesthesia
Small doses of dexmedetomidine1.5,3, 5µg used in combination with bupivacaine, in humans for spinal anesthesia has been shown to produce a more rapid onset of motor block, and a longer duration of motor and sensory block with…
- Trial name
- NCT03143010
- Testing
- intrathecal Dexmedetomidine, Dexmedetomidine 1.5 micrograms, Dexmedetomidine 3 micrograms
- Where
- Egypt
- Volunteers
- 200 people
- Sponsor
- Cairo University
Meniscus Disorder
Carotid Flow Time Measurement Guided Fluid Management During Spinal Anesthesia
Fluid management is a fundamental aspect of anesthesia. Several monitorization methods have been introduced to optimize fuid management. To date neither of them were ideal.
- Trial name
- NCT03734497
- Testing
- Group Carotis FTc 500 ml "Ringer's lactate" Lafleks®, Group Preloading 10 ml/kg "Ringer's lactate" Lafleks®, Group Control 2 ml/kg "Ringer's lactate" Lafleks®
- Where
- Turkey (Türkiye)
- Sponsor
- Diskapi Teaching and Research Hospital
Emergence Delirium
Emergence Delirium and Recovery Time in Children
In this study, inhalation anesthesia procedure and intravenous anesthesia method will be compared in terms of emergence delirium and recovery time in children who are scheduled for dental treatment under general anesthesia.
- Trial name
- NCT03330613
- Testing
- PAEDS, TIVA, Inhalational anesthesia
- Where
- Turkey (Türkiye)
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Aydin Adnan Menderes University
Anesthesia, Intubation
Impact of Extubation Location After Surgery on Perioperative Times
The additional time required to awaken a patient is one of the main reasons for not extubating him or her in the operating room (OR).
- Conditions
- Anesthesia, Intubation, Surgery, Extubation
- Trial name
- Extub_Loca (NCT06249659)
- Testing
- Extubation in operative room, Extubation in post anesthesia care unit
- Where
- France
- Volunteers
- 756 people
- Sponsor
- University Hospital, Clermont-Ferrand
Lung Cancer
Comparison of Emergence and Oxygenation During One-lung Ventilation With Desflurane and Propofol Anesthesia
Which is more adequate general anesthetic agent, desflurane or propofol, for emergence and recovery time, and perioperative oxygenation in lung resection surgery?
- Trial name
- NCT02324283
- Testing
- desflurane, propofol
- Where
- Japan
- Volunteers
- 80 people
- Sponsor
- Juntendo University
Anesthesia
The Effect of Sevofluorane on Wash-out Time in COPD
COPD (Chronic obstructive disease ) is a condition of respiratory system failure seen occasionally in elderly patients of society. Sevofluorane is a safe, volatile anesthetic used considerably widely all over the world.
- Trial name
- washout (NCT02209883)
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Duzce University
Postoperative Pain, Emergence Delirium
Effect of Preoperative Fasting Duration on Postoperative Pain and Emergence Agitation in Pediatric Patients Undergoing Urogenital Surgery
This study aims to evaluate the effect of preoperative fasting duration on postoperative pain and emergence agitation in pediatric patients undergoing urogenital surgery.
- Conditions
- Postoperative Pain, Emergence Delirium, Emergence Agitation
- Trial name
- NCT07552259
- Where
- Turkey (Türkiye)
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- TC Erciyes University
Discharge Time, Spinal Anesthesia
Regional Anesthesia in Ambulatory Endovenous Ablation Surgery
Varicose veins represent irreversible, abnormal dilatations of the venous structures. They manifest as tortuous, swollen vessels visible beneath the skin of the lower extremities, particularly the feet and legs.
- Conditions
- Discharge Time, Spinal Anesthesia, Ambulatory Surgery, Femoral Nerve Block
- Trial name
- NCT07297082
- Testing
- Femoral nerve block, Spinal anesthesia
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people
- Sponsor
- Ankara Etlik City Hospital
Laparoscopic Cholecystectomy
Effect of Caffeine on Time to Anesthetic Emergence After Laparoscopic Cholecystectomy : Randomized-controlled Trial
A faster emergence from general anesthesia has a double medico-economic impact by reducing the risks of complications and optimizing the performance of surgical units.
- Trial name
- NCT05079880
- Testing
- 300 mg of caffeine citrate infusion
- Where
- Tunisia
- Volunteers
- 60 people
- Sponsor
- Tunis University
Anesthesia
Oral Duloxetine as a Premedication for Postoperative Pain Control
The purpose of the study is to use duloxetine as premedication in Anterior cruciate ligament repair under spinal anesthesia and evaluate the effect on onset and duration of spinal anesthesia and postoperative pain control.
- Trial name
- NCT05050656
- Testing
- Duloxetine 60mg
- Where
- Egypt
- Volunteers
- 70 people
- Sponsor
- Ain Shams University
Postoperative Pain, Retinal Detachment
Postoperative Pain After Vitreoretinal Surgery
Postoperative pain (POP) is frequently underestimated in general and little data are available particularly for POP after vitreoretinal surgery (VRS).
- Trial name
- NCT03538847
- Testing
- Numerical rating scale
- Volunteers
- 800 people
- Sponsor
- University of Florence
Pulpotomies Primary Teeth
Effect of Local Anesthesia Techniques on Pulp Hemostasis in Primary Molars
The goal of this clinical trial is to compare the effects of two local anesthesia techniques on pulp hemostasis time during pulpotomy treatment of mandibular primary molars in children aged 6-9 years.
- Trial name
- NCT07810452
- Testing
- Inferior Alveolar Nerve Block Anesthesia, Computer-Controlled Intraosseous Anesthesia
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Afyonkarahisar Health Sciences University
MRI Sedation, Pediatric Sedation
Propofol-Only Versus Dexmedetomidine-Propofol in Children Undergoing Magnetic Resonance Imaging
The most common imaging procedure requiring sedation/anesthesia for the pediatric population is magnetic resonance imaging (MRI). However, the optimal anesthetic/sedation plan has not been determined for these procedures.
- Conditions
- MRI Sedation, Pediatric Sedation, Propofol Dosage, Emergence Delirium, Anesthesia
- Trial name
- NCT07369128
- Testing
- Dexmedetomidine (IV) 0.5 mcg/kg, Propofol (IV) 2-4 mg/kg, Dexmedetomidine (IV) 1 mcg/kg
- Where
- United States
- Volunteers
- 105 people
- Sponsor
- Boston Children's Hospital
POCD - Postoperative Cognitive Dysfunction, Recovery Time
The Effects of Anesthesia on Postoperative Cognitive Functions in Patients Undergoing Sleeve Gastrectomy
In this study, the investigators want to examine the effects of intravenous anesthetic drugs and gases on cognitive functions in the postoperative period in individuals who will undergo surgery for obesity.
- Conditions
- POCD - Postoperative Cognitive Dysfunction, Recovery Time, Postoperative Neurocognitive Disorder, Postoperative Delirium
- Trial name
- NCT07637357
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital